A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091096



Internal ID21289564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132918872..132921270hg38UCSC Ensembl
Innerchr11:132788767..132791165hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382399
hg192399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112570
Supporting Variants
Samplessample48
Known GenesOPCML
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091096
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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